A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7822855



Internal ID14539682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26564033..26564034hg38UCSC Ensembl
Innerchr10:26564016..26564051hg38UCSC Ensembl
Outerchr10:26564015..26564052hg38UCSC Ensembl
chr10:26852962..26852963hg19UCSC Ensembl
Innerchr10:26852945..26852980hg19UCSC Ensembl
Outerchr10:26852944..26852981hg19UCSC Ensembl
chr10:26892968..26892969hg18UCSC Ensembl
Innerchr10:26892986..26892951hg18UCSC Ensembl
Outerchr10:26892950..26892987hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38307
hg19307
hg18307
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3305653
Supporting Variants
SamplesNA18948
Known GenesAPBB1IP
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7822855
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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